Primary cutaneous B-cell lymphoblastic lymphoma in an elderly man.

The Korean Journal of Hematology Pub Date : 2011-12-01 Epub Date: 2011-12-27 DOI:10.5045/kjh.2011.46.4.283
Su-Yeon Cho, Seung-Sook Lee, Dae Hyun Back, Kyung Ah Lim, Ye Rim Lee, Hye Jin Kang
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引用次数: 3

Abstract

Precursor B-cell lymphoblastic lymphoma (B-LBL) is an uncommon high-grade neoplasm of immature B cells. It occurs predominantly in childhood with extranodal involvement such as skin and bone. Therefore, primary cutaneous involvement in elderly adults is a very rare manifestation of B-LBL. Here, we report a 78-year-old man with B-LBL presenting as a single cutaneous lesion which was immunohistochemically positive for leukocyte common antigen (LCA), CD79a, paired box 5 (PAX5), B cell lymphoma-2 (bcl-2), and terminal deoxynucleotidyl transferase (TdT) staining, but was without systemic involvement. The patient was treated using cyclophosphamide, adriamycin, vincristine, and prednisolone (CHOP), and achieved complete response (CR) at the first response assessment conducted after 3 CHOP cycles. After an additional cycle of CHOP treatment, radiotherapy was administered at a total dose of 3,600 cGy over 4 weeks. At the 21-month follow-up, he had maintained CR.

老年男性原发性皮肤b细胞淋巴母细胞淋巴瘤一例。
前体B细胞淋巴母细胞淋巴瘤(B- lbl)是一种罕见的未成熟B细胞高级别肿瘤。它主要发生在儿童期,并累及结外如皮肤和骨骼。因此,原发性皮肤受累在老年人中是一种非常罕见的B-LBL的表现。在这里,我们报告一位78岁的男性B- lbl患者,表现为单一皮肤病变,白细胞共同抗原(LCA), CD79a,配对盒5 (PAX5), B细胞淋巴瘤-2 (bcl-2)和末端脱氧核苷酸转移酶(TdT)染色免疫组化阳性,但没有全身累及。患者采用环磷酰胺、阿霉素、长春新碱、强的松龙(CHOP)治疗,3个CHOP周期后首次疗效评估达到完全缓解(CR)。在额外的CHOP治疗周期后,放射治疗的总剂量为3,600 cGy,超过4周。在21个月的随访中,他保持了CR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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